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Bipotent transitional liver progenitor cells contribute to liver regeneration
Following severe liver injury, when hepatocyte-mediated regeneration is impaired, biliary epithelial cells (BECs) can transdifferentiate into functional hepatocytes. However, the subset of BECs with such facultative tissue stem cell potential, as well as the mechanisms enabling transdifferentiation,...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group US
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10101857/ https://www.ncbi.nlm.nih.gov/pubmed/36914834 http://dx.doi.org/10.1038/s41588-023-01335-9 |
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author | Pu, Wenjuan Zhu, Huan Zhang, Mingjun Pikiolek, Monika Ercan, Caner Li, Jie Huang, Xiuzhen Han, Ximeng Zhang, Zhenqian Lv, Zan Li, Yan Liu, Kuo He, Lingjuan Liu, Xiuxiu Heim, Markus H. Terracciano, Luigi M. Tchorz, Jan S. Zhou, Bin |
author_facet | Pu, Wenjuan Zhu, Huan Zhang, Mingjun Pikiolek, Monika Ercan, Caner Li, Jie Huang, Xiuzhen Han, Ximeng Zhang, Zhenqian Lv, Zan Li, Yan Liu, Kuo He, Lingjuan Liu, Xiuxiu Heim, Markus H. Terracciano, Luigi M. Tchorz, Jan S. Zhou, Bin |
author_sort | Pu, Wenjuan |
collection | PubMed |
description | Following severe liver injury, when hepatocyte-mediated regeneration is impaired, biliary epithelial cells (BECs) can transdifferentiate into functional hepatocytes. However, the subset of BECs with such facultative tissue stem cell potential, as well as the mechanisms enabling transdifferentiation, remains elusive. Here we identify a transitional liver progenitor cell (TLPC), which originates from BECs and differentiates into hepatocytes during regeneration from severe liver injury. By applying a dual genetic lineage tracing approach, we specifically labeled TLPCs and found that they are bipotent, as they either differentiate into hepatocytes or re-adopt BEC fate. Mechanistically, Notch and Wnt/β-catenin signaling orchestrate BEC-to-TLPC and TLPC-to-hepatocyte conversions, respectively. Together, our study provides functional and mechanistic insights into transdifferentiation-assisted liver regeneration. |
format | Online Article Text |
id | pubmed-10101857 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group US |
record_format | MEDLINE/PubMed |
spelling | pubmed-101018572023-04-15 Bipotent transitional liver progenitor cells contribute to liver regeneration Pu, Wenjuan Zhu, Huan Zhang, Mingjun Pikiolek, Monika Ercan, Caner Li, Jie Huang, Xiuzhen Han, Ximeng Zhang, Zhenqian Lv, Zan Li, Yan Liu, Kuo He, Lingjuan Liu, Xiuxiu Heim, Markus H. Terracciano, Luigi M. Tchorz, Jan S. Zhou, Bin Nat Genet Article Following severe liver injury, when hepatocyte-mediated regeneration is impaired, biliary epithelial cells (BECs) can transdifferentiate into functional hepatocytes. However, the subset of BECs with such facultative tissue stem cell potential, as well as the mechanisms enabling transdifferentiation, remains elusive. Here we identify a transitional liver progenitor cell (TLPC), which originates from BECs and differentiates into hepatocytes during regeneration from severe liver injury. By applying a dual genetic lineage tracing approach, we specifically labeled TLPCs and found that they are bipotent, as they either differentiate into hepatocytes or re-adopt BEC fate. Mechanistically, Notch and Wnt/β-catenin signaling orchestrate BEC-to-TLPC and TLPC-to-hepatocyte conversions, respectively. Together, our study provides functional and mechanistic insights into transdifferentiation-assisted liver regeneration. Nature Publishing Group US 2023-03-13 2023 /pmc/articles/PMC10101857/ /pubmed/36914834 http://dx.doi.org/10.1038/s41588-023-01335-9 Text en © The Author(s) 2023, corrected publication 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Pu, Wenjuan Zhu, Huan Zhang, Mingjun Pikiolek, Monika Ercan, Caner Li, Jie Huang, Xiuzhen Han, Ximeng Zhang, Zhenqian Lv, Zan Li, Yan Liu, Kuo He, Lingjuan Liu, Xiuxiu Heim, Markus H. Terracciano, Luigi M. Tchorz, Jan S. Zhou, Bin Bipotent transitional liver progenitor cells contribute to liver regeneration |
title | Bipotent transitional liver progenitor cells contribute to liver regeneration |
title_full | Bipotent transitional liver progenitor cells contribute to liver regeneration |
title_fullStr | Bipotent transitional liver progenitor cells contribute to liver regeneration |
title_full_unstemmed | Bipotent transitional liver progenitor cells contribute to liver regeneration |
title_short | Bipotent transitional liver progenitor cells contribute to liver regeneration |
title_sort | bipotent transitional liver progenitor cells contribute to liver regeneration |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10101857/ https://www.ncbi.nlm.nih.gov/pubmed/36914834 http://dx.doi.org/10.1038/s41588-023-01335-9 |
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